8. Data Management

5. Investigator and Investigational Product

4. Regulatory Authority (RA)/Competent Authority (CA)

3. Ethics Committee (EC)/Institutional Review Board (IRB)

2. General Questions

11. Regulatory Overview - DCT Components

10. Roadmap of the Submission Process of a Clinical Trial

9. Subject Considerations

7. Decentralized Clinical Trials

6. Biological Specimen

1. Executive Summary